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Imaging single molecules in living cells for systems biology
In this work, I present the application of single-molecule imaging to systems biology and discuss the relevant technical issues within this context. Imaging single molecules has made it possible to visualize individual molecules at work in living cells. This continuously improving technique allows t...
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Formato: | Texto |
Lenguaje: | English |
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2006
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1682022/ https://www.ncbi.nlm.nih.gov/pubmed/17047663 http://dx.doi.org/10.1038/msb4100100 |
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author | Sako, Yasushi |
author_facet | Sako, Yasushi |
author_sort | Sako, Yasushi |
collection | PubMed |
description | In this work, I present the application of single-molecule imaging to systems biology and discuss the relevant technical issues within this context. Imaging single molecules has made it possible to visualize individual molecules at work in living cells. This continuously improving technique allows the measurement of non-invasively quantitative parameters of intracellular reactions, such as the number of molecules, reaction rate constants and diffusion coefficients with spatial distributions and temporal fluctuations. This detailed information about unitary intracellular reactions is essential for constructing quantitative models of reaction networks that provide a systems-level understanding of the mechanisms by which various cellular behaviors are emerging. |
format | Text |
id | pubmed-1682022 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
record_format | MEDLINE/PubMed |
spelling | pubmed-16820222007-01-25 Imaging single molecules in living cells for systems biology Sako, Yasushi Mol Syst Biol Review Article In this work, I present the application of single-molecule imaging to systems biology and discuss the relevant technical issues within this context. Imaging single molecules has made it possible to visualize individual molecules at work in living cells. This continuously improving technique allows the measurement of non-invasively quantitative parameters of intracellular reactions, such as the number of molecules, reaction rate constants and diffusion coefficients with spatial distributions and temporal fluctuations. This detailed information about unitary intracellular reactions is essential for constructing quantitative models of reaction networks that provide a systems-level understanding of the mechanisms by which various cellular behaviors are emerging. 2006-10-17 /pmc/articles/PMC1682022/ /pubmed/17047663 http://dx.doi.org/10.1038/msb4100100 Text en Copyright © 2006, EMBO and Nature Publishing Group |
spellingShingle | Review Article Sako, Yasushi Imaging single molecules in living cells for systems biology |
title | Imaging single molecules in living cells for systems biology |
title_full | Imaging single molecules in living cells for systems biology |
title_fullStr | Imaging single molecules in living cells for systems biology |
title_full_unstemmed | Imaging single molecules in living cells for systems biology |
title_short | Imaging single molecules in living cells for systems biology |
title_sort | imaging single molecules in living cells for systems biology |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1682022/ https://www.ncbi.nlm.nih.gov/pubmed/17047663 http://dx.doi.org/10.1038/msb4100100 |
work_keys_str_mv | AT sakoyasushi imagingsinglemoleculesinlivingcellsforsystemsbiology |